A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498638



Internal ID22556573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:95840150..95846124hg38UCSC Ensembl
chr4:96761301..96767275hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg385975
hg195975
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839904
Supporting Variants
Samples
Known GenesPDHA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498638
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer